Canonical Allele Identifier: PA141115
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47472
ClinVar RCV Id: RCV000040741 RCV000118786 RCV000476079 RCV001798191 RCV002354215
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg26775His
CA141113
NM_133378.4:c.80324G>A